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2.
Rev. esp. enferm. dig ; 114(12): 767-768, diciembre 2022. ilus
Article in Spanish | IBECS | ID: ibc-213553

ABSTRACT

El síndrome del conducto pancreático desconectado (SCPD) es debido a la interrupción del conducto pancreático (CP) principal o sus ramas secundarias, complicación presente entre un 30-80% de las pancreatitis agudas necrotizantes. La secreción de enzimas pancreáticas por el tejido pancreático aislado funcionante puede facilitar la recurrencia de colecciones necróticas encapsuladas, por lo que su manejo endoscópico sigue siendo un tema controvertido en la práctica diaria. Exponemos un caso de síndrome de ducto pancreático desconectado resuelto tras colocación de prótesis pancreática. (AU)


Subject(s)
Humans , Female , Middle Aged , Pancreatitis , Intensive Care Units , Patients , Gastrointestinal Tract
4.
Rev Esp Enferm Dig ; 114(12): 767-768, 2022 12.
Article in English | MEDLINE | ID: mdl-36281925

ABSTRACT

Disconnected pancreatic duct syndrome (DPCS) is due to disruption of the main pancreatic duct (PC) or its secondary branches, a complication present in 30-80% of acute necrotizing pancreatitis. The secretion of pancreatic enzymes by isolated functioning pancreatic tissue can facilitate the recurrence of encapsulated necrotic collections, so its endoscopic management remains a controversial issue in daily practice. We present a case of disconnected pancreatic duct syndrome resolved after placement of a pancreatic stent.


Subject(s)
Pancreatic Ducts , Pancreatitis, Acute Necrotizing , Humans , Pancreas , Pancreatitis, Acute Necrotizing/complications , Endoscopy , Drainage , Syndrome , Stents , Cholangiopancreatography, Endoscopic Retrograde
8.
Rev Esp Enferm Dig ; 114(4): 226-227, 2022 04.
Article in English | MEDLINE | ID: mdl-34315222

ABSTRACT

We report two cases of proctitis in men having sex with men.


Subject(s)
Lymphogranuloma Venereum , Proctitis , Homosexuality, Male , Humans , Male , Proctitis/diagnosis
10.
GE Port J Gastroenterol ; 28(4): 279-283, 2021 Jul.
Article in English | MEDLINE | ID: mdl-34386556

ABSTRACT

Strongyloides stercoralis is an intestinal nematode that colonizes and reproduces in the upper small intestinal mucosa. Infection in immunocompetent hosts is self-limited but in immunocompromised patients it can be complicated and cause hyperinfection. We present a 60-year-old female who was admitted due to an exacerbation of acquired thrombotic thrombocytopenic purpura requiring high doses of corticosteroids. The patient began to experience persistent pyrosis, nausea, vomiting, and oral intolerance. She was di-agnosed with syndrome of inappropriate secretion of antidiuretic hormone (SIADH). Upper endoscopy was performed and showed esophageal, gastric, and duodenal mucosa with edema and erythema. Moreover, there were superficial erosions and thickened folds in duodenum. Gastric and duodenal biopsies were taken. Abdominal computed tomography and magnetic enteroresonance displayed duodenal dilation and inflammatory changes. The histological study of biopsies showed colonization by S. stercolaris in the antrum and duodenum. S. stercolaris is a human parasite that is endemic in tropical, subtropical, and temperate regions. Its lifecycle is complex because it completes its entire cycle within the human host; it penetrates the skin, migrates to the lungs, and reach the gastrointestinal tract. The most affected site is the duodenum and upper jejunum. The lifecycle includes autoinfection through the intestinal mucosa or perianal skin, especially in immunocompromised hosts. Immunossuppression can lead to hyperinfection syndrome and disseminated disease. However, involvement of the stomach has relatively rarely been reported. SIADH has been related to systemic hyperinfection, although the mechanism is not clear. The relatively nonspecific clinical and imaging features and the low sensitivity of routine parasite tests make the diagnosis challenging and delayed.


Strongyloides stercoralis é um nematódo intestinal que coloniza e se reproduz na mucosa do intestino delgado proximal. A infeção em hospedeiros imunocompetentes é auto-limitada mas em doentes imunocomprometidos pode ter um curso complicado e causar hiperinfeção. Apresentamos um caso de uma mulher de 60 anos que é admitida devido a uma exacerbação de uma púrpura trombocitopénica trombótica adquirida com necessidade de altas doses de corticoides. A doente inicia quadro de pirose persistente, náuseas, vómitos e intolerância alimentar. Faz-se o diagnóstico de síndrome de secreção inapropriada de hormona antidiurética (SIADH). A endoscopia digestiva alta evidencia mucosa gástrica e duodenal com edema e eritema, para além de erosões e pregas espessadas duodenais. O TC e a enteroRMN mostram dilatação duodenal e alterações inflamatórias. A histologia mostra S. stercoralis a colonizar a mucosa do antro e duodeno. O S. stercolaris é um parasita humano, endémico em regiões tropicais e subtropicais. Tem um ciclo de vida complexo já que completa o seu ciclo todo dentro do organismo humano: penetra pela pele, migra para os pulmões e atinge o trato gastrointestinal. Os sítios mais afetados são o duodeno e o jejuno proximal. O ciclo de vida envolve autoinfeção na mucosa intestinal ou pele perianal, especialmente em doentes imunocomprometidos, com a imunodepressão podendo levar a síndrome de hiperinfeção e doença disseminada. Contudo, o envolvimento gástrico é raramente descrito. O SIADH tem sido relacionado com o síndrome de hiperinfeção, contudo, o seu mecanismo não é claro. O relativo inespecífico quadro clínico e alterações imagiológicas, assim como a baixa sensibilidade dos testes de parasitas de rotina atrasam e fazem o diagnóstico desafiante.

12.
Rev Esp Enferm Dig ; 113(5): 372-374, 2021 May.
Article in English | MEDLINE | ID: mdl-33406845

ABSTRACT

A 67-year-old female was referred due to epigastric pain, vomiting and weight loss of 6 kg in the past months. Blood tests were performed showing hematuria. An abdominal Doppler ultrasound did not show anything abnormal. Thus, an abdominal computed tomography (CT) angiography and a magnetic resonance imaging (MRI) enterography were performed, objectifying an aortomesenteric angle of 10.8° (reference range 38-56°), which caused a complete collapse of the left renal vein ("nutcracker phenomenon") and duodenal compression with retrograde dilatation ("Wilkie syndrome"). Conservative measures and nutritional support were adopted during hospitalization. She was discharged due to a good tolerance to an oral diet, the absence of symptoms and a good contrast pass in the esophagogastroduodenal transit.


Subject(s)
Renal Nutcracker Syndrome , Superior Mesenteric Artery Syndrome , Abdominal Pain/etiology , Aged , Duodenum , Female , Humans , Renal Nutcracker Syndrome/complications , Renal Nutcracker Syndrome/diagnostic imaging , Renal Veins/diagnostic imaging , Superior Mesenteric Artery Syndrome/complications , Superior Mesenteric Artery Syndrome/diagnostic imaging
14.
Rev Esp Enferm Dig ; 113(6): 477-478, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33267603

ABSTRACT

Lemmel's syndrome consists of obstructive jaundice due to compression of a periampular duodenal diverticulum (DDP), in the absence of choledocholithiasis or tumor. DDP are pseudodiverticula without a muscle layer within a radius of 2-3 centimeters from the ampulla of Vater. They rarely cause obstructive jaundice, although the prevalence is estimated at up to 22 % according to the sensitivity of the diagnostic test. They are usually incidental findings, but up to 1-5 % can be complicated with diverticulitis, bleeding, perforation, obstructive jaundice (Lemmel syndrome), choledocholithiasis, pancreatitis or cholangitis.


Subject(s)
Ampulla of Vater , Cholangitis , Diverticulum , Duodenal Diseases , Jaundice, Obstructive , Ampulla of Vater/diagnostic imaging , Ampulla of Vater/surgery , Diverticulum/complications , Diverticulum/diagnostic imaging , Duodenal Diseases/complications , Duodenal Diseases/diagnostic imaging , Humans , Jaundice, Obstructive/etiology
15.
Rev Esp Enferm Dig ; 113(3): 232, 2021 Mar.
Article in English | MEDLINE | ID: mdl-33222479

ABSTRACT

The case was an 86-year-old male with multiple cardiovascular comorbidites, including anticoagulated atrial fibrillation, who underwent a colonoscopy due to acute lower gastrointestinal bleeding and anemia. Colonoscopy only showed some small angiodysplasias in the cecum. A few hours later, the patient presented with abdominal pain and hemodynamic instability. An abdominal computed tomography was performed, which showed a splenic laceration and hemoperitoneum. An expectant attitude was decided, with a good evolution from the abdominal point of view. There was no sign of active splenic bleeding in a control computed tomography. However, he developed decompensated heart failure and finally died.


Subject(s)
Splenic Rupture , Aged, 80 and over , Colonoscopy , Hemoperitoneum/diagnostic imaging , Hemoperitoneum/etiology , Humans , Male , Splenectomy , Splenic Rupture/diagnostic imaging , Splenic Rupture/etiology , Splenic Rupture/surgery , Tomography, X-Ray Computed
16.
Rev Esp Enferm Dig ; 113(7): 549-550, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33244988

ABSTRACT

A 22-year-old male began with up to 12 loose stools per day, with mucus and no blood. They were present for two months, even during the night. Moreover, he complained of abdominal pain and weight loss. There were no findings on the blood tests. Fecal calprotectin was 225 µg/g. Stool microbiology tests were negative. Ileocolonoscopy displayed normal mucosa but the histological study of the biopsies showed Treponemas genus Brachispira. The patient had a sexual risk behavior. Treatment with metronidazole was initiated with clinical improvement.


Subject(s)
Gastrointestinal Microbiome , Adult , Diarrhea/drug therapy , Diarrhea/etiology , Feces , Humans , Intestines , Leukocyte L1 Antigen Complex , Male , Young Adult
17.
Rev Esp Enferm Dig ; 113(2): 149-150, 2021 Feb.
Article in English | MEDLINE | ID: mdl-33207897

ABSTRACT

We present the case of a 79-year-old male who underwent endoscopic retrograde cholangiopancreatography (ERCP) after cholangitis. The papilla was rigid and the biliary tract was dilated with sharpening of the distal bile duct, with no obvious cause. There was no bile flow after sphincterotomy, no stone after sweeping the duct with a balloon and the brush did not expand properly when trying to obtain cytologic material. Finally, a plastic stent was placed and purulent bile flowed. Biopsies of the papilla were taken due to the suspicion of tumor infiltration. The next day, the patient had pain in the right upper quadrant and blood tests highlighted mild anemization.


Subject(s)
Cholangiopancreatography, Endoscopic Retrograde , Liver Diseases , Aged , Cholangiopancreatography, Endoscopic Retrograde/adverse effects , Common Bile Duct , Gastrointestinal Hemorrhage , Hematoma/diagnostic imaging , Hematoma/etiology , Humans , Male , Sphincterotomy, Endoscopic
18.
Rev. esp. enferm. dig ; 112(12): 935-940, dic. 2020. tab
Article in Spanish | IBECS | ID: ibc-200583

ABSTRACT

En los últimos años se han venido realizando numerosos estudios sobre la función de la vitamina D en diversos procesos tanto fisiológicos como patológicos. Uno de los más interesantes se presenta en la Enfermedad inflamatoria intestinal, donde se ha observado una gran prevalencia de déficit de esta vitamina en los pacientes que la padecen. Este trabajo pretende revisar la literatura publicada hasta el momento y explicar su relación con la enfermedad, sus factores de riesgo, ponderar la importancia de la exposición solar, describir cómo afecta a los diversos tratamientos de la enfermedad o mostrar el efecto de la suplementación con vitamina en estos pacientes


No disponible


Subject(s)
Humans , Vitamin D/physiology , Vitamin D/therapeutic use , Inflammatory Bowel Diseases/therapy , Vitamin D Deficiency/epidemiology , Dietary Supplements , Sunlight/adverse effects , Vitamin D Deficiency/therapy , Polymerase Chain Reaction , Risk Factors , Avitaminosis/epidemiology , Fatigue
19.
Rev Esp Enferm Dig ; 112(12): 935-940, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33054287

ABSTRACT

In the last years,several studies have focused on the involement of vitamin D in different physiological and pathological processes. One of the most interesting actions occurs in the Inflammatory bowel disease, where a higher prevalence of vitamin D deficiency has been observed. This study aimed to review the literature in order to explain its relationship with the disease, the risk factors, measuring the importance of sun exposure, describing how treatments are affected or observing the effect of vitamin supplementation in this type of patients.


Subject(s)
Colitis , Inflammatory Bowel Diseases , Vitamin D Deficiency , Humans , Inflammatory Bowel Diseases/drug therapy , Inflammatory Bowel Diseases/epidemiology , Vitamin D , Vitamin D Deficiency/complications , Vitamin D Deficiency/epidemiology , Vitamins/therapeutic use
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